Publication | Open Access

Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib (sporPHP1B)

Similar FrequencyUrologyChromosome 20QMendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyCaucasian PatientsMedicineDisorders Of Sex DevelopmentClinical Genetics